| CPC A61F 2/82 (2013.01) [A61L 31/022 (2013.01); A61L 31/14 (2013.01); A61L 31/148 (2013.01); C22C 23/02 (2013.01); C22F 1/06 (2013.01)] | 13 Claims |

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1. A bioerodible endoprosthesis comprising:
a bioerodible magnesium alloy consisting of magnesium and between 5 and 11 weight percent aluminum, optionally between 0.1 and 3 weight percent zinc, optionally calcium, and optionally between 0.05 and 0.3 weight percent manganese, wherein the alloy has a microstructure comprising equiaxed Mg-rich solid solution phase grains having an average grain diameter of less than or equal to 5 microns and continuous or discontinuous second-phase precipitates in grain boundaries between the Mg-rich solid solution-phase grains, the second-phase precipitates having an average longest dimension of 0.5 micron or less, the bioerodible magnesium alloy including potential impurity elements of less than 200 ppm of each of iron, copper, nickel, cobalt, gold, cadmium, bismuth, sulfur, phosphorous, silicon, tin, lead and sodium.
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